反応式
[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5]/[CH:6]=[CH:7]\[CH2:8]/[CH:9]=[CH:10]\[CH:11]=[CH:12]\[CH:13]=[CH:14]\[C@@H:15]1[O:17][C@H:16]1[CH2:18][CH2:19][CH2:20][C:21]([OH:23])=[O:22].C(O)C(N)(CO)C[OH:27].Cl.[OH-].[Li+].CCCCC[C@H](O)/C=C/C1CCC(=O)C=1C/C=C\CCCC(O)=O>C(O)C>[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5]/[CH:6]=[CH:7]\[CH2:8][C@@H:9]([OH:27])/[CH:10]=[CH:11]/[CH:12]=[CH:13]/[CH:14]=[CH:15]\[C@@H:16]([OH:17])[CH2:18][CH2:19][CH2:20][C:21]([OH:23])=[O:22]参加物
実験手順
Leukotriene A4 hydrolase is determined by a direct enzyme assay of cytosolic fraction of cells treated with antisense oligonucleotides, as described by Ohishi et al. (J. Biol. Chem., 262:10200-10205, 1987). Briefly, HL-60 cells treated with antisense oligonucleotides are disrupted by sonication and cytosolic fraction isolated by centrifugation at 100,000× g for 1 hour. The reaction mixture contains 100 mM Tris-HCl buffer (pH=7.8) and enzyme in a total volume of 50 μL. After preincubating the enzyme for 3-4 minutes at 37° C., leukotriene A4 in ethanol containing lithium hydroxide was added to a final concentration of 75 μM and a final ethanol concentration of 2%. The enzyme was incubated for 1 minute at 37° C. and the reaction terminated by the addition of 100 μL of acetonitrile/methanol/acetic acid, 150:50:3 (v/v/v) containing 0.3 nmol prostaglandin B2 as an internal standard. Protein is precipitated by incubation at -20° C. for 30 minutes followed by centrifugation at 10,000× g for 10 minutes. A 120 μL aliquot of the supernatant was removed and 20 μL of 0.35% disodium EDTA is added. The amount of leukotriene B4 formed in 50 μL aliquot of the resulting solution is determined by reverse phase HPLC using a C18 column. Samples are eluted isocratically with solvent containing acetonitrile/methanol/water/acetic acid (3:1:3:0.006, v/v/v/v, 0.05% disodium EDTA). The absorbance at 270 nm is monitored to quantitate the amount of leukotriene B4 formed.
後処理
- customare disrupted by sonication and cytosolic fraction
- customisolated by centrifugation at 100,000× g for 1 hour
- customfor 3-4 minutes
- customat 37° C.
- additionwas added to a final concentration of 75 μM
- customthe reaction terminated by the addition of 100 μL of acetonitrile/methanol/acetic acid, 150:50:3 (v/v/v)
- customProtein is precipitated by incubation at -20° C. for 30 minutes
- waitg for 10 minutes
- customA 120 μL aliquot of the supernatant was removed
- addition20 μL of 0.35% disodium EDTA is added
出典と根拠
- ORDレコード
- ord-176853e43ca64abf8f2786a182a2f715
- 出典データセット
- uspto-grants-1996_06
- 特許番号
- US05530114
関連ノート
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